Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7068569

O=C(C[n+]1cccc(-c2cc(C(c3ccccc3)c3ccccc3)n[nH]2)c1)C1CC1.[Cl-]

nearest known ligand 0.35

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Hydrochloric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 1/20 0.35
APOBEC3A P31941 1/20 0.34
APOBEC3G Q9HC16 1/20 0.34
NPY5R Q15761 2/20 0.33
GSK3A P49840 8/20 0.33
GSK3B P49841 8/20 0.33
CDK2 P24941 1/20 0.31
ALDH1A1 P00352 2/20 0.31
KDM4E B2RXH2 1/20 0.31
LMNA P02545 1/20 0.31
TTK P33981 1/20 0.30
AURKB Q96GD4 1/20 0.30
INCENP Q9NQS7 1/20 0.30
CYP1A2 P05177 1/20 0.30
CYP2D6 P10635 1/20 0.30
HSP90AA1 P07900 1/20 0.30
USP30 Q70CQ3 1/20 0.30
NPC1 O15118 1/20 0.30
RAB9A P51151 1/20 0.30
SMN1; SMN2 Q16637 1/20 0.30

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Hydrochloric Acid SCHEMBL1194126 0.87 MAPK8 (0.38) KMT2AAPOBEC3AAPOBEC3GALDH1A1CYP2D6
SCHEMBL6597480 0.86 MAPK8 (0.39) KMT2AAPOBEC3AAPOBEC3GNPY5RALDH1A1
Hydrochloric Acid SCHEMBL1193657 0.85 KMT2A (0.44) KMT2AAPOBEC3AAPOBEC3GALDH1A1KDM4E
SCHEMBL6598021 0.83 KMT2A (0.45) KMT2AAPOBEC3AAPOBEC3GALDH1A1KDM4E
Hydrochloric Acid SCHEMBL6611866 0.80 POLB (0.38) KMT2AALDH1A1KDM4ELMNANPC1
SCHEMBL6599056 0.76 CYP3A4 (0.39) KMT2AAPOBEC3AAPOBEC3GALDH1A1LMNA
Hydrochloric Acid SCHEMBL5364641 0.76 KMT2A (0.35) KMT2AAPOBEC3AAPOBEC3GKDM4ECYP2D6
SCHEMBL6618821 0.74 MAPT (0.36) KMT2AALDH1A1KDM4ELMNARAB9A
SCHEMBL6598418 0.74 KMT2A (0.36) KMT2AAPOBEC3AAPOBEC3GKDM4ECYP2D6
Bromide SCHEMBL1194131 0.74 KMT2A (0.35) KMT2AAPOBEC3AAPOBEC3GKDM4ECYP2D6

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030045554-A1 Novel compounds for the management of aging-related and diabetic vascular complications, process for their preparation, therapeutic and cosmetic uses thereof TORRENT PHARMACEUTICALS LTD. 2003-03-06 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20030045554-A1 Novel compounds for the management of aging-related and diabetic vascular complications, process for their preparation, therapeutic and cosmetic uses thereof AGER, GLA, F12 KMT2A 3588/4885APOBEC3A 1017/4885APOBEC3G 1026/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.